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Reproduction of the Cape Horned Lizard, Phrynosoma coronatum (Squamata: Phrynosomatidae) from Baja California Sur, Mexico PDF

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Preview Reproduction of the Cape Horned Lizard, Phrynosoma coronatum (Squamata: Phrynosomatidae) from Baja California Sur, Mexico

1 Bull. SouthernCaliforniaAcad. Sci. 110(2).2011.pp.56-58 ©SouthernCaliforniaAcademyofSciences,201 Reproduction ofthe Gape Homed Lizard, Phrynosoma coronatum (Squamata: Phrynosomatidae) from Baja California Sur, Mexico Stephen R. Goldberg Whittier College, 13406 E. Philadelphia St. Whittier, CA 90608, [email protected] Species ofPhrynosoma (formerly P. coronatum) range west ofthe Sierra Nevada from Shasta County, California, south through southern California and Baja California (Grismer2002). Montanucci (2004) and Leacheetal. (2009)consideredPhrynosomafrom the southern tip of Baja California as P. coronatum. Goldberg (1983) reported on reproduction in Phrynosoma blainvillii (as P. coronatum) from southern California. To my knowledge, there is no information on reproduction ofP. coronatum from the Cape Region ofBaja Cahfornia Sur, Mexico. Thepurpose ofthis noteisto reporttheresultsof a histological examination of P. coronatum gonads from the Cape Region of Baja California Sur to ascertain whether geographic variation in reproduction exists between northern and southern species ofPhrynosoma (formerly P. coronatum, sensu Montanucci 2004, Leache et al. 2009). A sample of fourteen P. coronatum consisting of seven adult males (mean SVL = 76.9 mm ± 9.1 SD, range: 61-90 mm), five females (mean SVL = 79.2 mm ± 14.0 SD, range: 67-103 mm), one presumed neonate (SVL = 27 mm) and one presumed young of the year (SVL = 36 mm) was examined from the herpetology collection ofthe Natural History Museum of Los Angeles County (LACM), Los Angeles, California, U.S.A. (Appendix). Phrynosoma coronatum were collected 1964, 1967 and 1968. For histological examination, the left testiswas removed frommales and theleft ovary mm was removed from females. Enlarged follicles (> 5 length) were counted. Tissues were embedded in paraffin and cut into sections of5 |im. Slides were stained with Harris hematoxylin followed by eosin counterstain (Presnell and Schreibman 1997). Slides of testes were examined to determine the stage ofthe spermatogenic cycle. Slides ofovaries were examined for the presence of yolk deposition. An unpaired /-test was utilized to compare P. coronatum male and female mean body sizes (SVL) using Instat (vers. 3.0b, Graphpad Software, San Diego, CA). Histology slides were deposited in LACM. There was no significant size difference (mean SVL) between males and females ofP. coronatum (unpaired t test, / = 0.35, df = 10, P = 0.73). The only stage present in the testicular cycle was spermiogenesis (sperm formation) in which the lumina of the seminiferous tubules were lined by clusters ofsperm and/or metamorphosing spermatids. This condition was noted in the followingmonthly samples: (July, n = \; August, n = 6). The testes were previously removed leavingtheepididymidesin oneAugustmale (LACM 109380). Tubules ofthe epididymis were filled with sperm so it was assumed the missing seminiferous tubules were undergoing spermiogenesis. The smallest spermiogenic male (LACM 19904) measured 61 mm SVL and was from August. Monthly stages in the ovarian cycle are in Table 1. Three stages were noted: (1) quiescent, no yolk deposition; (2) early yolk deposition, basophilic yolk granules in the ooplasm: (3) enlarged ovarian follicles > 5 mm. One female from July (LACM 101500) 56 PHRYNOSOMA CORONATUMREPRODUCTION IN BAJA CALIFORNIA SUR 57 Table 1. Monthly stages in the ovarian cycle offive P. coronatum frorr1 Baja California Sur, Mexico. Month n Quiescent Earlyyolk deposition Enlarged follicles > 5 mm July 2 1 1 August 2 1 1 October 1 1 contained 12 enlarged follicles (> 5 mm) that would have ovulated later in the summer. This is within the range of7-16 clutch sizes reported by Goldberg (1983) for P. blainvilli (as P. coronatum) females from southern California. This was also the smallest reproductively active female (SVL = 71 mm). One female from August (LACM 19907) exhibited early yolk deposition which would have resulted in an egg clutch being produced during the coming autumn. One presumably neonate (LACM 101504, SVL = 27 mm) was collected 17 July and onejuvenile (LACM 19905, SVL = 36 mm) was collected 9 August both indicating P. coronatum commenced reproduction earlier in the year. My data indicate a significantly longer reproductive cycle for P. coronatum from the Cape Region ofBaja California Sur as compared to P. blainvillii in southern California (Goldberg 1983). Insouthern CaliforniaP. blainvillii(formerlyP. coronatum) isa "spring breeder" inwhichreproductiveactivitycommencesin March andends byJuly(Goldberg 1983). In the Cape Region of Baja California Sur, reproduction ofP. coronatum occurs through summer. Also, the appearance of a presumed neonate in July and a larger presumed young of the year in August suggest that P. coronatum commenced reproduction earlier in spring, perhaps concurrent with northern species ofPhrynosoma (sensu Montanucci 2004, Leache et al. 2009). Furthermore, winter activity has been reported for P. coronatum in the Cape Region (Vandenburgh 1895, Leviton and Banta (1964). In view of the extended reproductive season in the Cape Region, it appears femalesofP. coronatummayroutinelyproducetwoclutchesperseason, although thishas yetto be observed. Goldberg (1983) indicated two clutches might be possible for some P. blainvillii(asP. coronatum) femalesfrom southernCalifornia. In contrast, Howard (1974) reported one clutch was produced by Phrynosoma from northern Baja California. Acknowledgements I thank Christine Thacker (LACM) for permission to examine P. coronatum. Literature Cited Goldberg, S.R. 1983. Reproduction of the coast horned lizard, Phrynosoma coronatum, in southern California. Southwestern Naturalist, 28:478-479. Grismer, L.L. 2002. Amphibians and Reptiles of Baja California including its Pacific Islands and the islands in the Sea ofCortes. University ofCalifornia Press, Berkeley, xiii + 399 pp. Hovv'ard, W.R. 1974. Comparative reproductive ecology of horned lizards (Genus Phrynosoma) in southwestern United States and northern Mexico. Journal ofthe ArizonaAcademy ofScience, 9: 108-116. Leache,A.D.,M.S.Koo,C.L.Spencer,T.J.Papenfuss,R.N.Fisher,andJ.A. McGuire.2009.Quantifying ecological,morphological,andgeneticvariationtodelimitspeciesinthecoasthornedlizardspecies complex {Phrynosoma). Proceedings ofthe National Academy ofSciences, 106:12418-12423. Leviton,A.E.andB.H. Banta. 1964. MidwinterreconnaissanceoftheherpetofaunaoftheCapeRegionof BajaCalifornia,Mexico.ProceedingsoftheCaliforniaAcademyofScience,4"'series,330:127-156. 58 SOUTHERN CALIFORNIA ACADEMY OF SCIENCES Montanucci, R.R. 2004. Geographic variation in Phrynosoma coronatum (Lacertilia, Phrynosomatidae): further evidence for a peninsular archipelago. Herpetologica, 60:117-139. Presnell, J.K. and M.P. Schreibman. 1997. Humason's Animal Tissue Techniques. The Johns Hopkins University Press, Baltimore. 572 pp. Vanderburgh, J. 1895. Review of the herpetology of Lower California. Proceedings of the California Academy ofScience, 2:77-163. Appendix Phrynosoma coronatum from the Cape Region ofBaja California Sur examined from the herpetology collection of the Natural History Museum of Los Angeles County (LACM), LosAngeles, California U.S.A. (LACM 19903, 15 km E San Bartolo), (LACM 19904, 19905, 19906, vie. Santiago), (LACM 19907, 38 kmNW LaPaz), (LACM 101500, 101502, 101503, 101504, 101506, 109378, 109379, 109380, 109381, La Paz).

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